Pan paniscus (bonobo): 100986204
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Entry
100986204 CDS
T02283
Symbol
WNT9A
Name
(RefSeq) protein Wnt-9a
KO
K01064
wingless-type MMTV integration site family, member 9
Organism
pps
Pan paniscus (bonobo)
Pathway
pps04150
mTOR signaling pathway
pps04310
Wnt signaling pathway
pps04390
Hippo signaling pathway
pps04550
Signaling pathways regulating pluripotency of stem cells
pps04916
Melanogenesis
pps04934
Cushing syndrome
pps05010
Alzheimer disease
pps05022
Pathways of neurodegeneration - multiple diseases
pps05165
Human papillomavirus infection
pps05200
Pathways in cancer
pps05205
Proteoglycans in cancer
pps05217
Basal cell carcinoma
pps05224
Breast cancer
pps05225
Hepatocellular carcinoma
pps05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
pps00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
100986204 (WNT9A)
04390 Hippo signaling pathway
100986204 (WNT9A)
04150 mTOR signaling pathway
100986204 (WNT9A)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04550 Signaling pathways regulating pluripotency of stem cells
100986204 (WNT9A)
09150 Organismal Systems
09152 Endocrine system
04916 Melanogenesis
100986204 (WNT9A)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100986204 (WNT9A)
05205 Proteoglycans in cancer
100986204 (WNT9A)
09162 Cancer: specific types
05225 Hepatocellular carcinoma
100986204 (WNT9A)
05226 Gastric cancer
100986204 (WNT9A)
05217 Basal cell carcinoma
100986204 (WNT9A)
05224 Breast cancer
100986204 (WNT9A)
09172 Infectious disease: viral
05165 Human papillomavirus infection
100986204 (WNT9A)
09164 Neurodegenerative disease
05010 Alzheimer disease
100986204 (WNT9A)
05022 Pathways of neurodegeneration - multiple diseases
100986204 (WNT9A)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
100986204 (WNT9A)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
pps00536
]
100986204 (WNT9A)
Glycosaminoglycan binding proteins [BR:
pps00536
]
Heparan sulfate / Heparin
Morphogens
100986204 (WNT9A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
wnt
Motif
Other DBs
NCBI-GeneID:
100986204
NCBI-ProteinID:
XP_034804122
Ensembl:
ENSPPAG00000040433
LinkDB
All DBs
Position
1:21658115..21687710
Genome browser
AA seq
365 aa
AA seq
DB search
MLDGSPLARWLAAAFGLTLLLAALRPSAAYFGLTGSEPLTILPLTLEPEAAAQAHYKACD
RLKLERKQRRMCRRDPGVAETLVEAVSMSALECQFQFRFERWNCTLEGRYRASLLKRGFK
ETAFLYAISSAGLTHALAKACSAGRMERCTCDEAPDLENREAWQWGGCGDNLKYSSKFVK
EFLGRRSSKDLRARVDFHNNLVGVKVIKAGVETTCKCHGVSGSCTVRTCWRQLAPFHEVG
KHLKHKYETALKVGSTTNEAAGEAGAISPPRGRASGAGGSDPLPRTPELVHLDDSPSFCL
AGRFSPGTAGRRCHREKNCESICCGRGHNTQSRVVTRPCQCQVRWCCYVECRQCTQREEV
YTCKG
NT seq
1098 nt
NT seq
+upstream
nt +downstream
nt
atgctggatgggtccccgctggcgcgctggctggccgcggccttcgggctgacactgctg
ctcgccgcgctgcgcccttcggccgcctacttcgggctgacaggcagcgagcccctgacc
atcctcccgctgaccctggagccagaggcggccgcccaggcgcactacaaggcctgcgac
cggctgaagctggagcggaagcagcggcgcatgtgccgccgggacccgggcgtggcagag
acgctggtggaggccgtgagcatgagtgcgctcgagtgccagttccagttccgctttgag
cgctggaactgcacgctggagggccgctaccgggccagcctgctcaagcgaggcttcaag
gagactgccttcctctatgccatctcctcggctggcctgacgcacgcactggccaaggcg
tgcagcgcgggccgcatggagcgctgtacctgcgatgaggcgcccgacctggagaaccgt
gaggcctggcagtgggggggctgcggagacaaccttaagtacagcagcaagttcgtcaag
gaattcctgggcagacggtcaagcaaggatctgcgagcccgtgtggacttccacaacaac
ctcgtgggtgtgaaggtgatcaaggctggggtggagaccacctgcaagtgccatggcgtg
tcaggctcatgcacggtgcggacctgctggcggcagttggcgcctttccatgaggtgggc
aagcatctgaagcacaagtatgagacggcactcaaggtgggcagcaccaccaatgaagct
gccggcgaggcaggtgccatctccccaccacggggccgtgcctcgggggcaggcggcagc
gacccgctgccccgcactccagagctggtgcacctggatgactcgcctagcttctgcctg
gctggccgcttctccccgggcaccgctggccgtaggtgccaccgtgagaagaactgcgag
agcatctgctgcggccgcggccataacacacagagccgggtggtgacaaggccctgccag
tgccaggtgcgttggtgctgctatgtggagtgcaggcagtgcacgcagcgtgaggaggtc
tacacctgcaagggctga
DBGET
integrated database retrieval system